@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_head
{
this:
np:hasAssertion
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion
;
np:hasProvenance
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance
;
np:hasPublicationInfo
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion
a
np:Assertion
.
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance
a
np:Provenance
.
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion
{
miriam-gene:4089
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN71117e01fe250951e8040290d55bb422
sio:SIO_000628
miriam-gene:4089
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance
{
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion
dcterms:description
"[K-ras mutations frequently occur early, whereas changes in the expression and genetic integrity of the p16 gene appear in intermediate lesions, and the inactivation of the p53, DPC4 genes and activation of telomerase occur late in the neoplastic progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11490843
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}